WO2011134148A1 - Matériau luminescent à base de silicate et son procédé de production - Google Patents
Matériau luminescent à base de silicate et son procédé de production Download PDFInfo
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- WO2011134148A1 WO2011134148A1 PCT/CN2010/072286 CN2010072286W WO2011134148A1 WO 2011134148 A1 WO2011134148 A1 WO 2011134148A1 CN 2010072286 W CN2010072286 W CN 2010072286W WO 2011134148 A1 WO2011134148 A1 WO 2011134148A1
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- luminescent material
- silicate luminescent
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/08—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials
- C09K11/59—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing silicon
- C09K11/592—Chalcogenides
- C09K11/595—Chalcogenides with zinc or cadmium
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/08—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials
- C09K11/77—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing rare earth metals
- C09K11/7766—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing rare earth metals containing two or more rare earth metals
- C09K11/77742—Silicates
Definitions
- the invention belongs to the technical field of luminescent materials, and in particular relates to a silicate luminescent material and a preparation method thereof.
- luminescent materials have always been one of the hotspots for people to compete in research and development.
- organic electroluminescent materials for example, organic electroluminescent materials, photoluminescent materials, cathode ray-excited luminescent materials, ultraviolet-excited luminescent materials. These different luminescent materials can be applied to respective illumination and display devices, etc., respectively.
- a plasma flat panel display is a novel direct view image display device following a cathode ray tube and a liquid crystal display.
- Plasma flat panel display has the advantages of active illumination, high brightness, large viewing angle, high contrast, good color reproduction, rich grayscale and fast response. It has become an important large-screen high-definition flat panel display technology.
- the principle of illuminating the plasma display panel is that it is discharged by an inert gas such as Xe or Xe-He, and becomes a plasma state, and emits vacuum ultraviolet rays of 147 nm and 172 nm.
- the ultraviolet ray excites the phosphor coated on the inner wall to emit red, green, and blue.
- the primary color light can be color-displayed by spatial color mixing and circuit control.
- Zn 2 SiO 4 :Mn 2+ is the most commonly used green phosphor in plasma flat panel displays. Under vacuum ultraviolet excitation, Zn 2 SiO 4 :Mn 2+ has excellent brightness and excellent resistance to degradation. Very bright saturation. However, the afterglow time of Zn 2 SiO 4 :Mn 2+ is too long, which is disadvantageous for a picture that is quickly displayed. Further, since the dielectric constant of Zn 2 SiO 4 :Mn 2+ is higher than that of the red and blue phosphors for a plasma display panel, a higher induced voltage is required when driving a display device such as a plasma display panel.
- This new green phosphor is mainly a Mn 2+ -activated aluminate such as BaMgAl 10 O 17 :Mn 2+ phosphor, Ba 0.9 Mg 0.6 Mn 0.16 ⁇ 8Al 2 O 3 green phosphor, and the like. These new green phosphors have a lower dielectric constant. However, due to the use of Mn2+ as an activator, such green phosphors have a longer afterglow time, and such phosphors also have lower luminance.
- a silicate luminescent material having a short afterglow and a high luminance is provided.
- a silicate luminescent material having a chemical formula of Re 4-x Tb x MgSi 3 O 13 , wherein Re is at least one element selected from the group consisting of Y, Gd, La, Lu, and Sc, and 0.05 ⁇ x ⁇ 1 .
- the source compound of each element is selected according to a molar ratio in the chemical formula Re 4-x Tb x MgSi 3 O 13 , wherein Re is at least one element selected from the group consisting of Y, Gd, La, Lu, and Sc, 0.05 ⁇ X ⁇ 1;
- the calcined product is calcined in a reducing atmosphere, cooled and ground to obtain the silicate luminescent material.
- the silicate luminescent material has a short afterglow time of about 2.13 ms, which is much lower than commercial Zn 2 SiO 4 :Mn 2+ ;
- the silicate luminescent material is based on Re 4 MgSi 3 O 13 and is doped with Tb ions.
- the matrix has strong absorption of vacuum ultraviolet light and is activated by Tb ions to make the luminescent material in vacuum ultraviolet Strong green light emission under light excitation;
- silicate luminescent material is very stable, and its performance is basically unchanged after being treated by blisters, high-temperature heating, and the like;
- the preparation method of the silicate luminescent material can be obtained mainly by pre-baking and roasting treatment, and the process is simple, easy to realize industrialization, and has broad production and application prospects.
- FIG. 1 is a flow chart of a method for preparing a silicate luminescent material according to an embodiment of the present invention
- Figure 2 is an emission spectrum of the silicate luminescent material of Example 6 of the present invention, the excitation wavelength is 172 nm;
- Figure 3 is an excitation spectrum of the silicate luminescent material of Example 6 of the present invention, the monitoring wavelength is 543 nm;
- Fig. 4 is a graph showing the fluorescence decay curve of the silicate luminescent material of Example 6 of the present invention.
- the silicate luminescent material of the embodiment of the invention has a chemical formula of Re 4-x Tb x MgSi 3 O 13 , wherein Re is at least one element selected from the group consisting of Y, Gd, La, Lu, and Sc, 0.05 ⁇ x ⁇ 1.
- Re is two or more elements selected from the group consisting of Y, Gd, La, Lu, and Sc, for example, a combination of Y and Gd, and a combination of four elements of Y, Gd, La, and Lu, and by the combination of these different elements, With higher optical properties of different elements, higher luminosity can be obtained.
- x is from 0.1 to 0.5, and a suitable amount of Tb ion doping can be obtained.
- the silicate luminescent material In the above silicate luminescent material, Re 4 MgSi 3 O 13 is used as a matrix, and Tb ions are doped, the matrix has strong absorption to vacuum ultraviolet light, and the activation of Tb ions makes the luminescent material in vacuum ultraviolet It has a strong green light emission under light excitation, and thus has a higher light-emitting brightness.
- the silicate luminescent material absorbs energy through the matrix under the excitation of vacuum ultraviolet light, and is transmitted to the luminescent center Tb ions, and the green light emission is generated by the Tb ions.
- the silicate luminescent material has strong absorption at 147 nm and 172 nm, thereby improving its luminescence intensity, and is suitably applied to devices such as plasma display panels.
- the silicate luminescent material has a short afterglow time of about 2.13 ms, which is much lower than commercial Zn 2 SiO 4 :Mn 2+ ;
- the silicate luminescent material is based on Re 4 MgSi 3 O 13 and is doped with Tb ions.
- the matrix has strong absorption of vacuum ultraviolet light and is activated by Tb ions to make the luminescent material in vacuum ultraviolet Strong green light emission under light excitation;
- silicate luminescent material is very stable, and its performance is basically unchanged after being treated by blisters, high-temperature heating, and the like.
- a flow chart of a method for preparing a silicate luminescent material according to an embodiment of the present invention includes the following steps:
- the source compound of Re is preferably at least one of an oxide, a carbonate, an oxalate, and a nitrate
- the source compound of Tb is preferably an oxide or a carbonic acid thereof.
- the source compound of magnesium is at least one of magnesium oxide, magnesium carbonate, magnesium oxalate, and magnesium nitrate
- the source compound of silicon is silica.
- x is preferably from 0.1 to 0.5.
- Step S02 includes the steps of: adding boric acid to a mixture of source compounds of the above elements, and grinding and mixing them, and the amount of boric acid added is Re 4-x Tb x MgSi 3 O 13 molar amount (or can be calculated as Mg ion) The molar amount is 0.5 to 5%.
- the specific procedure of mixing is as follows: After adding boric acid, the mixture is sufficiently ground in a mortar, uniformly mixed, and then subjected to step S03.
- Step S03 specifically includes a process of pre-baking a mixture of source compounds of each element in an air atmosphere at a temperature of 1000 to 1400 ° C for 1 to 8 hours.
- the prebaking temperature is preferably from 1100 to 1300 ° C, and the prebaking time is preferably from 2 to 6 hours.
- Step S04 specifically includes the following steps: grinding the product of the calcination treatment, and calcining at a temperature of 1100 to 1500 ° C for 1 to 8 hours under a reducing atmosphere.
- the temperature at the time of baking is preferably 1250 to 1400
- the calcination time is preferably 2 to 6 hours.
- the calcination temperature is higher than the prebaking temperature, for example, about 100 to 350 ° C, and the total time of prebaking and calcination is preferably 5 to 12 hours.
- the reducing atmosphere may be an atmosphere formed by a nitrogen gas and a hydrogen mixed gas, a carbon monoxide gas or hydrogen gas having a volume ratio of 95:5.
- the above prebaking treatment may also be referred to as heat treatment, and the calcination treatment may also be referred to as sintering treatment.
- the calcined product may be further ground into a powder and sieved to form a phosphor of a certain particle size.
- the silicate luminescent material can be obtained by the calcination and the calcination treatment, and the whole preparation process is simple and the cost is low.
- compositions of the silicate luminescent materials and methods for their preparation, as well as their properties, etc. are exemplified below by way of various examples.
- Example 1 Green phosphor composed of Y 3.95 Tb 0.05 MgSi 3 O 13
- Example 4 Green phosphor composed of Gd 3.2 Tb 0.8 MgSi 3 O 13
- Example 7 Green phosphor composed of La 1.5 Sc 0.5 Lu 1.5 Tb 0.5 MgSi 3 O 13
- Example 8 Green phosphor composed of Y 3 Lu 0.3 Tb 0.7 MgSi 3 O 13
- the mixture was sintered at 1500 ° C for 2 hours under a 95% N 2 + 5% H 2 weak reducing atmosphere, cooled to room temperature, and after grinding, a white product was obtained, which was a YLaGdLu 0.5 Tb 0.5 MgSi 3 O 13 green phosphor.
- Example 10 Green phosphor composed of Y 3.6 Gd 0.1 Sc 0.1 Tb 0.2 MgSi 3 O 13
- the Y 3 Gd 0.5 Tb 0.5 MgSi 3 O 13 luminescent material of Example 6 was exemplified below, and its excitation spectrum, emission spectrum, and fluorescence decay were tested to illustrate the luminescent properties of the luminescent material of the present invention.
- the emission spectrum of the Y 3 Gd 0.5 Tb 0.5 MgSi 3 O 13 luminescent material obtained in the above Example 6 is shown.
- the luminescent material prepared in Example 6 is emitted at 172 nm excitation, which has a strong absorption peak at around 543 nm, and the integrated intensity of the emission spectrum is high, indicating that the material has strong luminescence properties, and has a higher luminescence property. High brightness.
- the excitation spectrum of the Y 3 Gd 0.5 Tb 0.5 MgSi 3 O 13 luminescent material obtained in the above Example 6 is shown.
- the Y 3 Gd 0.5 Tb 0.5 MgSi 3 O 13 luminescent material has a strong absorption of ultraviolet light of about 172 nm, indicating that it has good absorption in the vacuum ultraviolet band.
- the fluorescence decay curve of the Y 3 Gd 0.5 Tb 0.5 MgSi 3 O 13 luminescent material obtained in the above Example 6 is shown.
- the figure shows that the afterglow time of the material is 2.13ms, which is much lower than the afterglow time of the current commercial green powder.
- the afterglow time of the Zn 2 SiO 4 :Mn 2+ material is 7.1ms, indicating that it has a short afterglow. Low fluorescence lifetime.
- the afterglow time of the silicate luminescent material is short, about 2.13 ms, which is much lower than the commercial Zn 2 SiO 4 :Mn 2+ and is excited by vacuum ultraviolet light. There is a strong green light emission.
- the silicate luminescent material can be obtained by the pre-baking and roasting treatment, thereby making the preparation process simple, the cost low, and having a broad production and application prospect.
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- Organic Chemistry (AREA)
- Luminescent Compositions (AREA)
Abstract
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US13/638,668 US9045690B2 (en) | 2010-04-28 | 2010-04-28 | Silicate luminescent material and production method thereof |
EP10850481.2A EP2565253B1 (fr) | 2010-04-28 | 2010-04-28 | Matériau luminescent à base de silicate et son procédé de production |
PCT/CN2010/072286 WO2011134148A1 (fr) | 2010-04-28 | 2010-04-28 | Matériau luminescent à base de silicate et son procédé de production |
JP2013505301A JP2013525525A (ja) | 2010-04-28 | 2010-04-28 | ケイ酸塩発光材料及びその製造方法 |
CN2010800642287A CN102770507A (zh) | 2010-04-28 | 2010-04-28 | 硅酸盐发光材料及其制备方法 |
Applications Claiming Priority (1)
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PCT/CN2010/072286 WO2011134148A1 (fr) | 2010-04-28 | 2010-04-28 | Matériau luminescent à base de silicate et son procédé de production |
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WO2011134148A1 true WO2011134148A1 (fr) | 2011-11-03 |
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PCT/CN2010/072286 WO2011134148A1 (fr) | 2010-04-28 | 2010-04-28 | Matériau luminescent à base de silicate et son procédé de production |
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US (1) | US9045690B2 (fr) |
EP (1) | EP2565253B1 (fr) |
JP (1) | JP2013525525A (fr) |
CN (1) | CN102770507A (fr) |
WO (1) | WO2011134148A1 (fr) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN116875308A (zh) * | 2023-07-17 | 2023-10-13 | 中国科学院长春应用化学研究所 | 发光材料及其制备方法、led光源 |
CN116891741A (zh) * | 2023-07-12 | 2023-10-17 | 陕西学前师范学院 | 一种宽带黄绿色荧光粉及其制备方法 |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
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CN112390647B (zh) * | 2019-08-12 | 2023-05-05 | 中国科学院宁波材料技术与工程研究所 | 一种紫外激发实现光谱拓展的核壳荧光陶瓷粉体及其制备方法 |
CN112426367A (zh) * | 2020-12-11 | 2021-03-02 | 西安邮电大学 | 用于齿科的可标记发光修复材料及制备方法、粘结剂及制备方法和修复结构 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
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US5951915A (en) * | 1996-01-22 | 1999-09-14 | Kasei Optonix, Ltd. | Phosphorescent phosphor |
CN1470597A (zh) * | 2003-07-07 | 2004-01-28 | 中国科学院长春应用化学研究所 | 硅酸盐发光薄膜的制备方法 |
CN101077973A (zh) * | 2006-05-26 | 2007-11-28 | 大连路明发光科技股份有限公司 | 硅酸盐荧光材料及其制造方法以及使用其的发光装置 |
Family Cites Families (3)
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JP4713169B2 (ja) | 2005-01-25 | 2011-06-29 | 国立大学法人鳥取大学 | 蛍光体 |
US20090315448A1 (en) * | 2005-04-07 | 2009-12-24 | Sumitomo Chemical Company, Limited | Phosphor, phosphor paste and light emitting device |
TWI378138B (en) | 2007-04-02 | 2012-12-01 | Univ Nat Chiao Tung | Green-emitting phosphors and process for producing the same |
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2010
- 2010-04-28 US US13/638,668 patent/US9045690B2/en active Active
- 2010-04-28 WO PCT/CN2010/072286 patent/WO2011134148A1/fr active Application Filing
- 2010-04-28 JP JP2013505301A patent/JP2013525525A/ja active Pending
- 2010-04-28 CN CN2010800642287A patent/CN102770507A/zh active Pending
- 2010-04-28 EP EP10850481.2A patent/EP2565253B1/fr not_active Not-in-force
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5951915A (en) * | 1996-01-22 | 1999-09-14 | Kasei Optonix, Ltd. | Phosphorescent phosphor |
CN1470597A (zh) * | 2003-07-07 | 2004-01-28 | 中国科学院长春应用化学研究所 | 硅酸盐发光薄膜的制备方法 |
CN101077973A (zh) * | 2006-05-26 | 2007-11-28 | 大连路明发光科技股份有限公司 | 硅酸盐荧光材料及其制造方法以及使用其的发光装置 |
Non-Patent Citations (1)
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See also references of EP2565253A4 * |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN116891741A (zh) * | 2023-07-12 | 2023-10-17 | 陕西学前师范学院 | 一种宽带黄绿色荧光粉及其制备方法 |
CN116891741B (zh) * | 2023-07-12 | 2024-04-19 | 陕西学前师范学院 | 一种宽带黄绿色荧光粉及其制备方法 |
CN116875308A (zh) * | 2023-07-17 | 2023-10-13 | 中国科学院长春应用化学研究所 | 发光材料及其制备方法、led光源 |
Also Published As
Publication number | Publication date |
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CN102770507A (zh) | 2012-11-07 |
EP2565253A1 (fr) | 2013-03-06 |
EP2565253B1 (fr) | 2016-08-24 |
US9045690B2 (en) | 2015-06-02 |
EP2565253A4 (fr) | 2013-03-06 |
JP2013525525A (ja) | 2013-06-20 |
US20130020534A1 (en) | 2013-01-24 |
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